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使用脂质体纳米颗粒抑制血小板功能可阻止肿瘤转移。

Inhibition of platelet function using liposomal nanoparticles blocks tumor metastasis.

作者信息

Zhang Yinlong, Wei Jingyan, Liu Shaoli, Wang Jing, Han Xuexiang, Qin Hao, Lang Jiayan, Cheng Keman, Li Yiye, Qi Yingqiu, Anderson Greg J, Sukumar Saraswati, Li Suping, Nie Guangjun

机构信息

College of Pharmaceutical Science, Jilin University, Changchun 130021, China.

CAS Key Laboratory for Biomedical Effects of Nanomaterials & Nanosafety, CAS Center for Excellence in Nanoscience, National Center for Nanoscience and Technology, Beijing 100190, China.

出版信息

Theranostics. 2017 Feb 26;7(5):1062-1071. doi: 10.7150/thno.17908. eCollection 2017.

Abstract

Extensive evidence has shown that platelets support tumor metastatic progression by inducing epithelial-mesenchymal transition of cancer cells and by shielding circulating tumor cells from immune-mediated elimination. Therefore, blocking platelet function represents a potential new avenue for therapy focused on eliminating metastasis. Here we show that liposomal nanoparticles bearing the tumor-homing pentapeptide CREKA (Cys-Arg-Glu-Lys-Ala) can deliver a platelet inhibitor, ticagrelor, into tumor tissues to specifically inhibit tumor-associated platelets. The drug-loaded nanoparticles (CREKA-Lipo-T) efficiently blocked the platelet-induced acquisition of an invasive phenotype by tumor cells and inhibited platelet-tumor cell interaction . Intravenously administered CREKA-Lipo-T effectively targeted tumors within 24 h, and inhibited tumor metastasis without overt side effects. Thus, the CREKA-Lipo formulation provides a simple strategy for the efficient delivery of anti-metastatic drugs and shows considerable promise as a platform for novel cancer therapeutics.

摘要

大量证据表明,血小板通过诱导癌细胞的上皮-间质转化以及保护循环肿瘤细胞免受免疫介导的清除来支持肿瘤转移进展。因此,阻断血小板功能代表了一种专注于消除转移的潜在新治疗途径。在此我们表明,携带肿瘤归巢五肽CREKA(半胱氨酸-精氨酸-谷氨酸-赖氨酸-丙氨酸)的脂质体纳米颗粒可以将血小板抑制剂替格瑞洛递送至肿瘤组织,以特异性抑制肿瘤相关血小板。载药纳米颗粒(CREKA-Lipo-T)有效地阻断了血小板诱导的肿瘤细胞侵袭表型的获得,并抑制了血小板与肿瘤细胞的相互作用。静脉注射CREKA-Lipo-T在24小时内有效地靶向肿瘤,并抑制肿瘤转移且无明显副作用。因此,CREKA-Lipo制剂为抗转移药物的有效递送提供了一种简单策略,并作为新型癌症治疗平台显示出巨大前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2353/5399576/956798ef4e05/thnov07p1062g001.jpg

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